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胶束电动毛细管色谱法测定金果榄中古伦宾和蝙蝠葛任碱的含量
引用本文:崔小敏,刘有平,王 鑫,周秋红,邸 欣. 胶束电动毛细管色谱法测定金果榄中古伦宾和蝙蝠葛任碱的含量[J]. 沈阳药科大学学报, 2012, 29(9): 689-692
作者姓名:崔小敏  刘有平  王 鑫  周秋红  邸 欣
作者单位:沈阳药科大学 药学院,辽宁 沈阳 110016
摘    要:目的建立测定金果榄药材中古伦宾和蝙蝠葛任碱含量的胶束电动毛细管色谱法。方法采用未涂层熔融石英毛细管柱(35.2 cm×50μm I.D.,有效长度为26.9 cm),运行缓冲液为20 mmol.L-1硼酸溶液(含200 mmol.L-1十二烷基硫酸钠,pH值8.0)-异丙醇-甲醇(体积比70∶20∶10),分离电压为18 kV,检测波长为210 nm,压力自动进样。结果古伦宾和蝙蝠葛任碱的线性范围分别为0.210~1.68 g.L-1和0.026~0.21 g.L-1,线性关系良好。平均加样回收率分别为100.5%和96.1%,RSD分别为3.4%和3.6%(n=6)。应用该法测定10批金果榄药材中古伦宾和蝙蝠葛任碱的含量。结论该方法准确、可靠、环保,适用于金果榄中古伦宾和蝙蝠葛任碱的同时含量测定。

关 键 词:金果榄  古伦宾  蝙蝠葛任碱  胶束电动毛细管色谱  含量测定
收稿时间:2012-03-13
修稿时间:2012-05-13

Determination of columbin and menisperine in Tinosporae Radix by micellar electrokinetic capillary chromatography
CUI Xiao-min,LIU You-ping,WANG Xin,ZHOU Qiu-hong,DI Xin. Determination of columbin and menisperine in Tinosporae Radix by micellar electrokinetic capillary chromatography[J]. Journal of Shenyang Pharmaceutical University, 2012, 29(9): 689-692
Authors:CUI Xiao-min  LIU You-ping  WANG Xin  ZHOU Qiu-hong  DI Xin
Affiliation:School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China
Abstract:Objective To develop a micellar electrokinetic capillary chromatographic method for the determination of columbin and menisperine in Tinosporae Radix. Methods Separation was carried out in an uncoated fused-silica capillary (35.2 cm × 50 μm I.D., 26.9 cm effective length) using 20 mmol·L-1 boric acid (pH 8.0)-isopropanol-methanol(V:V:V =70:20:10)as running buffer at 18 kV. The detection wavelength was set at 210 nm. Results The linear ranges of columbin and menisperine were 0.210-1.68 g·L-1 and 0.026-0.21 g·L-1, respectively. The average recoveries of columbin and menisperine were 100.5% and 96.1%, and the relative standard deviations (RSDs) were less than 3.6% (n=6). Conclusion The method is simple and economical and can be applied for the determination of columbin and menisperine in Tinosporae Radix.
Keywords:Tinosporae Radix  columbin  menisperine  micellar electrokinetic capillary chromatography  content determination
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